"GeneDx"[submitter] AND "LOC130060467"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 60134	GRCh38/hg38 17p11.2(chr17:18828089-20467764)x3	AKAP10, ALDH3A1 +91 more	Copy number gain	See cases	GUncertain significance
Select item 60135	GRCh38/hg38 17p11.2(chr17:19070690-21619442)x3	AKAP10, ALDH3A1 +116 more	Copy number gain	See cases	GUncertain significance
Select item 1302060	NM_000382.3(ALDH3A2):c.153+223C>G	ALDH3A2, LOC130060467	Single nucleotide variant (intron variant)	not provided	GLikely benign

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